Title: Sr. CRA 2, FSP - Invitro Diagnostics - East Coast, Midwest & West Coast Location: Remote United States time type Full time job requisition id 261209 Job Description: Our FSP team is currently seeking Sr. CRA 2s with 4+ years of monitoring residing in the East Coast, Midwest & West Coast US! WHAT YOU WILL DO You will utilize your skills, knowledge, and clinical judgement to provide a high standard of care for participants in clinical trials and respond to emergency situations based upon clinical research standards. Responsibilities: - Responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of pre-study and initiation visits; liaise with vendors; and other duties, as assigned - - Responsible for all aspects of site management as prescribed in the project plans - General On-Site Monitoring - Ensure the study staff who will conduct the protocol have received the proper materials and instructions to safely enter patients into the study - Ensure the protection of study patients by verifying that informed consent procedures and protocol requirements are adhered to according to the applicable regulatory requirements - Ensure the integrity of the data submitted on Case Report Forms (CRFs) or other data collection tools by careful source document Monitor data for missing or implausible data - Responsible for all aspects of registry management as prescribed in the project plans - Undertake feasibility work when requested - Complete Serious Adverse Event (SAE) reporting, process production of repo11s, narratives and follow up of SAEs - Independently perform CRF review; query generation and resolution against established data review guidelines on Fortrea or client data management systems as assigned by management - Assist with training of new employees, eg. co-monitoring - Coordinate designated clinical projects as a Local Project Coordinator (with supervision, if applicable) and may act as a local client contact as assigned - Perform other duties as assigned by management Requirements - University or college degree, or certification in a related allied health profession from an appropriately accredited institution (e.g. nursing licensure) - 4+ years of Clinical Monitoring experience - 50-60% overnight travel The important thing for us is you are comfortable working in an environment that is: - Fast paced: where no deviations from the study protocol are allowed, and not meeting a timeline for even few minutes will create a quality issue. - Changing priorities constantly asking you to prioritize and adapt on the spot. - Teamwork and people skills are essential for the study to run smoothly. - Technology based. We collect our data directly into an electronic environment. Work Environment: - Work is performed in an office environment with exposure to electrical office equipment. - Frequent travel to clients/ site locations with occasional travel both domestic and international. Physical Requirements: - Ability to sit for extended periods and operate a vehicle safely. - Repetitive hand movement of both hands with the ability to make fast, simple, repeated movements of the fingers, hands, and wrists. - Occasional crouching, stooping, with frequent bending and twisting of upper body and neck. - Ability to access and use a variety of computer software developed both in-house and off-the-shelf. - Light to moderate lifting and carrying (or otherwise moves) objects including luggage and laptop computer with a maximum lift of 15-20 lbs. - Regular and consistent attendance. - Varied hours may be required. - Target Pay Range: $125 - $140K #LI - Remote Applications will be accepted on an ongoing basis.

• Assist with preparing proposals, protocols, and reports by conducting internet and literature searches. • Conduct literature reviews by abstracting data from scientific articles. • Participate in and oversee site recruitment, site contracting and IRB submissions, site management, and site training (including tracking enrollment and scheduling). • Manage data, including performing data entry and review. Assist with data analysis, including preparing qualitative code books, performing and overseeing coding, and reviewing quantitative data tables. Conduct one-on-one cognitive interviews and co-moderating focus groups; compile data collection tools. Handle data extraction (epidemiological and clinical data); model programming (larger parts of models). • Perform efficient delegation and communication within and outside of the project team. • Assist with financial management. • Provide scientific support in the implementation of simulation models (e.g., discrete event simulation) and other decision-analytic models (e.g., Markov, individual state-transition, survival partition) to assess the cost-effectiveness of healthcare interventions. • Assist project managers on multiple projects including drafting sections of project deliverables (reports, dossiers, protocols, spreadsheets, etc.) and participate in abstract, manuscript preparation, project proposals (e.g., gathering relevant material, drafting background sections, conducting scoping searches, and developing project budgets). • Participate in client meetings and prepare meeting minutes.

Title: Psychologist Location: Wetumpka, Alabama, United States Department: Mental Health Job Description: NaphCare is hiring a Psychologist to join our team of medical professionals at the Julia Tutwiler Prison located in Wetumpka, Alabama. As a Correctional Psychologist, you will provide psychological treatment and support to the facility residents while working alongside correctional officers and other medical professionals. This is a unique position where you can make a difference to this diverse population of patients with complex mental health needs. Responsibilities The Psychologist is responsible for providing psychological leadership, consultation and direct services for patients to help improve their mental health and reduce the risk of recidivism. Additional responsibilities may include and not be limited to: - Collaborating with a multidisciplinary team in providing assessment and treatment of mental and emotional disorders of patients. - Working with inmates to prepare them for reintegration into society, providing support for finding housing, employment, and other resources. - Providing counseling and support to help inmates manage emotional challenges, cope with incarceration, and develop coping mechanisms. - Coordinating, leading and participating in educational training activities related to mental health care - Conducting risk assessments to identify potential dangers to inmates and the public, informing decisions about housing, treatment, and release Qualifications Experience / Requirements / Qualifications - Must hold a current, unrestricted Psychologist license in AL - Must possess an active BLS/CPR Certification (AHA preferred) - Experience with underserved and marginalized populations, including those with mental health and substance use disorders - Strong communication skills and ability to communicate with diverse individuals, including other medical professionals, correctional staff and judges - Ability to interpret and analyze data to create treatment plans - Knowledge of applicable laws, regulations, and industry standards - Able to maintain confidentiality of all proprietary and/or confidential information - Display integrity, professionalism and be able to adhere to a Code of Conduct and comply with all facility(s) correctional healthcare policies, procedures, and legal requirements - Must pass the facility’s criminal background check and drug screening Why Join NaphCare? NaphCare is one of the largest providers of healthcare services to correctional facilities throughout the US and we are growing. If you have never considered a career in correctional healthcare, now may be the time. In addition to competitive salaries and generous employee benefits, we strongly support career advancement within the company. NaphCare Benefits for Full-Time Employees Include: - Health, dental & vision insurance that starts day one! - Prescriptions free of charge through our health plan, beginning day one! - Lowest Cost Benefits! - Employee Assistance Program (EAP) services - 401K and Roth with company contribution that starts day one! - Tuition Assistance - Referral bonuses - Term life insurance at no cost to the employee - Generous paid time off & paid holidays - Free continuing education and CMEs NaphCare has a partnership with NetCE that provides CEU/CME for our staff. NetCE uses a rigorous peer review process to ensure that all activities and content are up to date. This service streamlines continuing education for all NaphCare Employees to meet state specific requirements for maintaining licensing. If you would like to speak with me to learn more about this position and NaphCare, apply directly to the position to initiate the application process, and I’ll be in touch.

• Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards. • Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution. • Collaborating with cross-functional teams to ensure timely and accurate data collection and reporting. • Providing training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct. • Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations.